6533b824fe1ef96bd1281417

RESEARCH PRODUCT

Efficacy and acceptability of pharmacological and non-pharmacological interventions for non-specific chronic low back pain: a protocol for a systematic review and network meta-analysis

Nicola VeroneseLucy MarshSharon Marie WeldonSharon Marie WeldonMarco SolmiBrendon StubbsAndrea CiprianiAndrea CiprianiClaire RossatoJohn P. A. IoannidisSofia DiasElena DragiotiJoseph FirthJoseph FirthDamian PoulterTrevor ThompsonJae Il ShinChristopher G. Maher

subject

Adultmedicine.medical_specialtyPsychological interventionMEDLINEMedicine (miscellaneous)lcsh:Medicinenot knownlaw.inventionRS03 medical and health sciences0302 clinical medicineQuality of life (healthcare)Randomized controlled trialMeta-Analysis as TopiclawmedicineProtocolHumansLow back pain030212 general & internal medicineFunctional abilityNetwork meta-analysisExercisebusiness.industrylcsh:RBayes TheoremLow back painClinical trialRandomized controlled trialMeta-analysisPhysical therapySystematic reviewQuality of Lifemedicine.symptombusiness030217 neurology & neurosurgerySystematic Reviews as Topic

description

Abstract Background Despite the enormous financial and humanistic burden of chronic low back pain (CLBP), there is little consensus on what constitutes the best treatment options from a multitude of competing interventions. The objective of this network meta-analysis (NMA) is to determine the relative efficacy and acceptability of primary care treatments for non-specific CLBP, with the overarching aim of providing a comprehensive evidence base for informing treatment decisions. Methods We will perform a systematic search to identify randomised controlled trials of interventions endorsed in primary care guidelines for the treatment of non-specific CLBP in adults. Information sources searched will include major bibliographic databases (MEDLINE, Embase, CENTRAL, CINAHL, PsycINFO and LILACS) and clinical trial registries. Our primary outcomes will be patient-reported pain ratings and treatment acceptability (all-cause discontinuation), and secondary outcomes will be functional ability, quality of life and patient/physician ratings of overall improvement. A hierarchical Bayesian class-based NMA will be performed to determine the relative effects of different classes of pharmacological (NSAIDs, opioids, paracetamol, anti-depressants, muscle relaxants) and non-pharmacological (exercise, patient education, manual therapies, psychological therapy, multidisciplinary approaches, massage, acupuncture, mindfulness) interventions and individual treatments within a class (e.g. NSAIDs: diclofenac, ibuprofen, naproxen). We will conduct risk of bias assessments and threshold analysis to assess the robustness of the findings to potential bias. We will compute the effect of different interventions relative to placebo/no treatment for both short- and long-term efficacy and acceptability. Discussion While many factors are important in selecting an appropriate intervention for an individual patient, evidence for the analgesic effects and acceptability of a treatment are key factors in guiding this selection. Thus, this NMA will provide an important source of evidence to inform treatment decisions and future clinical guidelines. Systematic review registration PROSPERO registry number: CRD42019138115

10.1186/s13643-020-01398-3http://europepmc.org/articles/PMC7275431